Pages that link to "Q42950808"
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The following pages link to About the "Asian"-specific 9-bp deletion of mtDNA.... (Q42950808):
Displaying 6 items.
- Major genomic mitochondrial lineages delineate early human expansions (Q21093396) (← links)
- Molecular instability in the COII-tRNA(Lys) intergenic region of the human mitochondrial genome: multiple origins of the 9-bp deletion and heteroplasmy for expanded repeats. (Q35212075) (← links)
- Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. (Q35238441) (← links)
- Mutational analysis of the mitochondrial tRNA genes and flanking regions in umbilical cord tissue from uninfected infants receiving AZT-based therapies for prophylaxis of HIV-1. (Q35327135) (← links)
- mtDNA control-region sequence variation suggests multiple independent origins of an "Asian-specific" 9-bp deletion in sub-Saharan Africans. (Q35881549) (← links)
- The 9-bp deletion in region V of mtDNA: a risk factor of hearing loss and encephalomyopathy in Caucasian populations? (Q43811835) (← links)